CLASS I ONGOING Device recall · Reported 19 Feb 2025 · FDA Enforcement Report

Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial recalled

Max Mobility is recalling Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial, distributed in 44 states. The recall was initiated on 20 Dec 2024 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesAll serial numbers manufactured between August 17,2023 through November 21, 2024
Quantity recalledunknown

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-1117-2025
FDA event ID
96086
Recalling firm
Max Mobility, Lebanon, TN
Classification
Class I
Status
Ongoing
Recall initiated
20 Dec 2024
FDA classified
11 Feb 2025
Reported
19 Feb 2025
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Other Reasons

Timeline

20 Dec 2024Recall initiated by company
11 Feb 2025Classified by FDA+53 days
19 Feb 2025Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Due to faulty circuit board in speed control remote use in conjunction with a wheelchair power assist, their is a potential for lost of control of device potentially resulting in minor and major injuries.

Product as listed by the FDA

Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCK use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.

Where it was distributed

US: AK AL AR AZ CA CO CT DC DE FL GA HI IA ID IL IN KS KY LA MA MD ME MI MN MO MS MT NC ND NE NH NJ NM NV NY OH OK OR PA PR RI SC SD TN TX UT VA VT WA WI WV WY OUS: Sweden, Canada, Australia, Japan, New Zealand, Colombia, Argentina, Hong Kong, Canada, Mexico, Bermuda, South Korea, Chile

AlaskaAlabamaArkansasArizonaCaliforniaColoradoConnecticutDistrict of ColumbiaFloridaGeorgiaIowaIllinoisKansasKentuckyLouisianaMassachusettsMarylandMichiganMinnesotaMissouri

Questions about this recall

Why was it recalled?

Due to faulty circuit board in speed control remote use in conjunction with a wheelchair power assist, their is a potential for lost of control of device potentially resulting in minor and major injuries.

Which lots are affected?

All serial numbers manufactured between August 17,2023 through November 21, 2024

Where was it sold?

US: AK AL AR AZ CA CO CT DC DE FL GA HI IA ID IL IN KS KY LA MA MD ME MI MN MO MS MT NC ND NE NH NJ NM NV NY OH OK OR PA PR RI SC SD TN TX UT VA VT WA WI WV WY OUS: Sweden, Canada, Australia, Japan, New Zealand, Colombia, Argentina, Hong Kong, Canada, Mexico, Bermuda, South Korea, Chile

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 96086

This product is part of a recall event; the main page for the event is Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial recalled.

ReportedClassRecallCompanyReasonWhere
CLASS IMax Mobility/Permobil Smart Drive MX2+ SpeedControl Dial recalledMax MobilityOther44 states

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